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Bianca Haase

dblp:158/8454 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2015
0000-0001-6493-9808ORCID · reported

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › genomics
genotyping
0.212015
Simple, rapid and accurate genotyping-by-sequencing from aligned whole genomes with ArrayMaker · Bioinform. 2015
Bioinformatics and computational biology › genomics › genotyping
genotyping-by-sequencing
0.212015
Simple, rapid and accurate genotyping-by-sequencing from aligned whole genomes with ArrayMaker · Bioinform. 2015
Bioinformatics and computational biology › genomics
genome-wide association study
0.112015
Simple, rapid and accurate genotyping-by-sequencing from aligned whole genomes with ArrayMaker · Bioinform. 2015

Methods — techniques the papers use, named apart from their topics

whole-genome alignment · 0.2
YearPublicationVenuePosition
2015 Simple, rapid and accurate genotyping-by-sequencing from aligned whole genomes with ArrayMaker
abstract
SUMMARY: Whole-genome sequencing has revolutionized the study of genetics. Genotyping-by-sequencing is now a viable method of genotyping, yet the bioinformatics involved can be daunting if not prohibitive for some laboratories. Here we present ArrayMaker, a user-friendly tool that extracts accurate single nucleotide polymorphism genotypes at pre-defined loci from whole-genome alignments and presents them in a standard genotyping format compatible with association analysis software and datasets genotyped on commercial array platforms. Using this tool, geneticists with only basic computing ability can genotype samples at any desired list of markers, facilitating genome-wide association analysis, fine mapping, candidate variant assessment, data sharing and compatibility of data sourced from multiple technologies. AVAILABILITY AND IMPLEMENTATION: ArrayMaker is licensed under The MIT License and can be freely obtained at https://github.com/cw2014/ArrayMaker/. The program is implemented in Perl and runs on Linux operating systems. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. CONTACT: [email protected].
Cali E. Willet, Bianca Haase, Michael A. Charleston, Claire M. Wade
Bioinform.2